2′-Deoxyuridine 3′-Monophosphate

Status : experimental

Chemical Classification

This compound belongs to the class of organic compounds known as pyrimidine 2′-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.

Pyrimidine 2′-deoxyribonucleosides

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrimidine nucleosides

Pyrimidine 2′-deoxyribonucleosides

Calculated Property

kind Value Source
logP -1.6 ALOGPS
logS -1.6 ALOGPS
Water Solubility 8.41e+00 g/l ALOGPS
logP -1.6 ChemAxon
IUPAC Name {[(2R,3S,5R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-2-(hydroxymethyl)oxolan-3-yl]oxy}phosphonic acid ChemAxon
Traditional IUPAC Name 3′-dUMP ChemAxon
Molecular Weight 308.1819 ChemAxon
Monoisotopic Weight 308.040951914 ChemAxon
SMILES OC[C@H]1O[C@H](C[C@@H]1OP(O)(O)=O)N1C=CC(=O)NC1=O ChemAxon
Molecular Formula C9H13N2O8P ChemAxon
InChI InChI=1S/C9H13N2O8P/c12-4-6-5(19-20(15,16)17)3-8(18-6)11-2-1-7(13)10-9(11)14/h1-2,5-6,8,12H,3-4H2,(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1 ChemAxon
InChIKey InChIKey=LXKGKXYIAAKOCT-SHYZEUOFSA-N ChemAxon
Polar Surface Area (PSA) 145.63 ChemAxon
Refractivity 61.93 ChemAxon
Polarizability 25.63 ChemAxon
Rotatable Bond Count 4 ChemAxon
H Bond Acceptor Count 7 ChemAxon
H Bond Donor Count 4 ChemAxon
pKa (strongest acidic) 1.09 ChemAxon
pKa (strongest basic) -3 ChemAxon
Physiological Charge -2 ChemAxon
Number of Rings 2 ChemAxon
Bioavailability 1 ChemAxon
Rule of Five 1 ChemAxon
Ghose Filter 0 ChemAxon
MDDR-Like Rule 0 ChemAxon

Target within organism

  • Ribonuclease 4 : in Human
  • Ribonuclease pancreatic : in Human